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表现为组织学上与弓形虫淋巴结炎无法区分的传染性单核细胞增多症淋巴结炎。三例报告。

Infectious mononucleosis lymphoadenitis showing histologic findings indistinguishable from toxoplasma lymphadenitis. A report of three cases.

机构信息

Department of Anatomic and Diagnostic Pathology, Dokkyo Medical University School of Medicine, Mibu, Tochigi 321-0293, Japan.

出版信息

Pathol Res Pract. 2010 Jun 15;206(6):361-4. doi: 10.1016/j.prp.2009.12.010. Epub 2010 Feb 23.

Abstract

Lymph node lesions in infectious mononucleosis (IM) show a marked histologic diversity. We report here three cases of IM lymphadenitis with histologic findings indistinguishable from those of toxoplasmic lymphadenitis. The histologic findings of the three cases presented here showed a histologic triad of toxoplasmic lymphadenitis, including (i) numerous lymphoid follicles with hyperplastic germinal centers; (ii) small clusters or single epithelioid histiocytes; and (iii) multiple foci of monocytoid B-cells. Moreover, all three lesions contained isolated or small clusters of epithelioid histiocytes within the hyperplastic germinal centers and the periphery of lymphoid follicles, which are the most specific histologic findings of toxoplasmic lymphadenitis. However, serologic findings confirmed EBV infection in all three cases. On in situ hybridization, numerous Epstein-Barr virus (EBV)-encoded small RNA (EBER)-positive cells were demonstrated in the germinal center, as well as in interfollicular areas in all three cases. Toxoplasmosis gondii infection was excluded in at least one case, based on serologic findings. Polymerase chain reaction analysis also demonstrated that there was no T. gondii DNA in the remaining two cases. Two of our three cases showed atypical clinical presentations, including an absence of atypical lymphocytosis in peripheral blood in two cases, age more than 30 years, and an absence of systemic symptoms in one case. It appears that previous descriptions emphasize the differential diagnostic problems between IM lymphadenitis and malignant lymphomas. However, from a therapeutic perspective, it is important to discriminate IM lymphadenitis from toxoplasmic lymphadenitis particularly in patients showing atypical clinical features.

摘要

传染性单核细胞增多症(IM)的淋巴结病变表现出明显的组织学多样性。我们在此报告三例 IM 淋巴结炎,其组织学表现与弓形虫淋巴结炎无法区分。这三例的组织学发现表现为弓形虫淋巴结炎的组织学三联征,包括(i)大量具有增生性生发中心的淋巴滤泡;(ii)小簇或单个上皮样组织细胞;和(iii)多个单核细胞 B 细胞灶。此外,所有三个病变均在增生性生发中心和淋巴滤泡的外围中包含孤立或小簇的上皮样组织细胞,这是弓形虫淋巴结炎最具特异性的组织学发现。然而,血清学发现证实了这三个病例均存在 EBV 感染。原位杂交显示,在所有三个病例的生发中心以及滤泡间区均有大量 Epstein-Barr 病毒(EBV)编码的小 RNA(EBER)阳性细胞。在至少一个病例中,基于血清学发现排除了弓形体感染。聚合酶链反应分析也表明,在其余两个病例中没有 T. gondii DNA。我们的三个病例中有两个表现出非典型临床表现,包括两个病例外周血中无异型淋巴细胞,一个病例年龄大于 30 岁,一个病例无全身症状。似乎之前的描述强调了 IM 淋巴结炎和恶性淋巴瘤之间的鉴别诊断问题。然而,从治疗的角度来看,区分 IM 淋巴结炎和弓形虫淋巴结炎尤为重要,特别是在表现出非典型临床特征的患者中。

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